Works matching IS 13899600 AND DT 2008 AND VI 7
Results: 51
Delivering cancer genetics services-new ways of working.
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- 2008
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- Publication type:
- Correction Notice
Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas.
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- Familial Cancer, 2008, v. 7, n. 4, p. 319, doi. 10.1007/s10689-008-9194-8
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- Publication type:
- Article
Cascade genetic testing for mismatch repair gene mutations.
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- Familial Cancer, 2008, v. 7, n. 4, p. 293, doi. 10.1007/s10689-008-9192-x
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- Article
Mutation spectrum in HNPCC in the Israeli population.
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- Familial Cancer, 2008, v. 7, n. 4, p. 309, doi. 10.1007/s10689-008-9191-y
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- Article
Predictors of choosing life-long screening or prophylactic surgery in women at high and moderate risk for breast and ovarian cancer.
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- Familial Cancer, 2008, v. 7, n. 4, p. 347, doi. 10.1007/s10689-008-9189-5
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- Article
The three nucleotide deletion within the 3′untranslated region of MLH1 resulting in gene expression reduction is not a causal alteration in Lynch syndrome.
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- 2008
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- Publication type:
- Letter
Working through a diagnostic challenge: colonic polyposis, Amsterdam criteria, and a mismatch repair mutation.
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- Familial Cancer, 2008, v. 7, n. 4, p. 281, doi. 10.1007/s10689-007-9179-z
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- Article
Predicting breast cancer risk: implications of a “weak” family history.
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- Familial Cancer, 2008, v. 7, n. 4, p. 361, doi. 10.1007/s10689-008-9197-5
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- Article
Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.
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- Familial Cancer, 2008, v. 7, n. 4, p. 331, doi. 10.1007/s10689-008-9195-7
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- Publication type:
- Article
Screen positive rates among six family history screening protocols for breast/ovarian cancer in four cohorts of women.
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- Familial Cancer, 2008, v. 7, n. 4, p. 341, doi. 10.1007/s10689-008-9188-6
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- Publication type:
- Article
Family history and colorectal cancer survival in women.
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- Familial Cancer, 2008, v. 7, n. 4, p. 287, doi. 10.1007/s10689-008-9190-z
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- Publication type:
- Article
Screening for urinary tract cancer with urine cytology in Lynch syndrome and familial colorectal cancer.
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- Familial Cancer, 2008, v. 7, n. 4, p. 303, doi. 10.1007/s10689-008-9193-9
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- Publication type:
- Article
8th International Symposium on von Hippel-Lindau Disease.
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- Familial Cancer, 2008, v. 7, p. S13, doi. 10.1007/s10689-008-9211-y
- Publication type:
- Article
The Inaugural Birt-Hogg-Dubé (BHD) Symposium.
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- Familial Cancer, 2008, v. 7, p. S1, doi. 10.1007/s10689-008-9210-z
- Publication type:
- Article
Probability estimation models for prediction of BRCA1 and BRCA2 mutation carriers: COS compares favourably with other models.
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- Familial Cancer, 2008, v. 7, n. 3, p. 199
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- Publication type:
- Article
Prolactin and systemic malignancies: a close association.
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- Familial Cancer, 2008, v. 7, n. 3, p. 265, doi. 10.1007/s10689-008-9185-9
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- Publication type:
- Article
Influence of germline polymorphisms of GSTT1 , GSTM1 , and GSTP1 in familial versus sporadic breast cancer susceptibility and survival.
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- Familial Cancer, 2008, v. 7, n. 3, p. 213, doi. 10.1007/s10689-007-9177-1
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- Publication type:
- Article
Family history of cancer in Brazil: is it being used?
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- Familial Cancer, 2008, v. 7, n. 3, p. 229, doi. 10.1007/s10689-008-9180-1
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- Publication type:
- Article
Psychological and cancer-specific distress at 18 months post-testing in women with demonstrated BRCA1 mutations for hereditary breast/ovarian cancer.
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- Familial Cancer, 2008, v. 7, n. 3, p. 245
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- Publication type:
- Article
Inequality of use of Cancer Genetics Services by members of breast, ovarian and colorectal cancer families in South East Scotland.
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- Familial Cancer, 2008, v. 7, n. 3, p. 259, doi. 10.1007/s10689-008-9184-x
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- Publication type:
- Article
Muir-Torre Syndrome: expanding the genotype and phenotype—a further family with a MSH6 mutation.
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- Familial Cancer, 2008, v. 7, n. 3, p. 255, doi. 10.1007/s10689-008-9183-y
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- Publication type:
- Article
Use of association studies to define genetic modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.
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- Familial Cancer, 2008, v. 7, n. 3, p. 233, doi. 10.1007/s10689-008-9181-0
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- Publication type:
- Article
The extracolonic cancer spectrum in females with the common ‘South African’ hMLH1 c.C1528T mutation.
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- Familial Cancer, 2008, v. 7, n. 3, p. 191
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- Publication type:
- Article
Prolactin levels, breast-feeding and milk production in a cohort of young healthy women from high-risk breast cancer families: implications for breast cancer risk.
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- Familial Cancer, 2008, v. 7, n. 3, p. 221, doi. 10.1007/s10689-007-9178-0
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- Publication type:
- Article
Sessile serrated polyps of the colorectum are rare in patients with Lynch syndrome and in familial colorectal cancer families.
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- Familial Cancer, 2008, v. 7, n. 2, p. 157
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- Publication type:
- Article
Prevalence of BRCA1 and BRCA2 mutations in breast cancer patients from Cuba.
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- Familial Cancer, 2008, v. 7, n. 3, p. 275, doi. 10.1007/s10689-008-9187-7
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- Publication type:
- Article
Gonadal mosaicism and familial adenomatous polyposis.
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- Familial Cancer, 2008, v. 7, n. 2, p. 173, doi. 10.1007/s10689-007-9169-1
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- Publication type:
- Article
Loss of heterozygosity at 19p13.2 and 2q21 in tumours from familial clusters of non-medullary thyroid carcinoma.
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- Familial Cancer, 2008, v. 7, n. 2, p. 141
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- Publication type:
- Article
Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC).
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- Familial Cancer, 2008, v. 7, n. 2, p. 163
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- Publication type:
- Article
Tumor histology helps to identify Lynch syndrome among colorectal cancer patients.
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- Familial Cancer, 2008, v. 7, n. 3, p. 267, doi. 10.1007/s10689-008-9186-8
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- Publication type:
- Article
Is MSH2 a breast cancer susceptibility gene?
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- Familial Cancer, 2008, v. 7, n. 2, p. 151
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- Publication type:
- Article
Sebaceous adenomas in an MYH associated polyposis patient of Indian (Gujarati) origin.
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- Familial Cancer, 2008, v. 7, n. 2, p. 187, doi. 10.1007/s10689-007-9161-9
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- Article
Cancer risk reduction and reproductive concerns in female BRCA1/2 mutation carriers.
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- Familial Cancer, 2008, v. 7, n. 2, p. 179, doi. 10.1007/s10689-007-9171-7
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- Publication type:
- Article
A novel MSH2 germline mutation in a Druze HNPCC family.
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- Familial Cancer, 2008, v. 7, n. 2, p. 135
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- Article
Characterization of the pathogenic mechanism of a novel BRCA2 variant in a Chinese family.
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- Familial Cancer, 2008, v. 7, n. 2, p. 125
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- Article
BRCA1/2 mutation analysis in male breast cancer families from North West England.
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- Familial Cancer, 2008, v. 7, n. 2, p. 113, doi. 10.1007/s10689-007-9153-9
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- Publication type:
- Article
Familial breast cancer: double heterozygosity for BRCA1 and BRCA2 mutations with differing phenotypes.
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- Familial Cancer, 2008, v. 7, n. 2, p. 119, doi. 10.1007/s10689-007-9154-8
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- Publication type:
- Article
Standards of care in diagnosis and testing for hereditary colon cancer.
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- Familial Cancer, 2008, v. 7, n. 1, p. 65, doi. 10.1007/s10689-007-9159-3
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- Article
Hereditary diffuse gastric cancer: association with lobular breast cancer.
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- Familial Cancer, 2008, v. 7, n. 1, p. 73
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- Publication type:
- Article
Hereditary colorectal cancer syndromes: molecular genetics, genetic counseling, diagnosis and management.
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- Familial Cancer, 2008, v. 7, n. 1, p. 27, doi. 10.1007/s10689-007-9165-5
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- Publication type:
- Article
Pancreatic cancer and the FAMMM syndrome.
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- Familial Cancer, 2008, v. 7, n. 1, p. 103, doi. 10.1007/s10689-007-9166-4
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- Publication type:
- Article
A hereditary cancer syndrome seminar: perspective of a Continuing Medical Education (CME) Director.
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- Familial Cancer, 2008, v. 7, n. 1, p. 3, doi. 10.1007/s10689-007-9170-8
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- Article
Foreword.
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- Familial Cancer, 2008, v. 7, n. 1, p. 1, doi. 10.1007/s10689-007-9168-2
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- Publication type:
- Article
Genetic counseling and clinical management of newly diagnosed breast cancer patients at genetic risk for BRCA germline mutations: perspective of a surgical oncologist.
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- Familial Cancer, 2008, v. 7, n. 1, p. 91, doi. 10.1007/s10689-007-9167-3
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- Publication type:
- Article
Chemoprevention with special reference to inherited colorectal cancer.
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- Familial Cancer, 2008, v. 7, n. 1, p. 59, doi. 10.1007/s10689-007-9158-4
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- Publication type:
- Article
Hereditary neoplasia syndromes and the role of the surgeon.
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- Familial Cancer, 2008, v. 7, n. 1, p. 97, doi. 10.1007/s10689-007-9156-6
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- Publication type:
- Article
Hereditary gynecologic cancers: differential diagnosis, surveillance, management and surgical prophylaxis.
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- Familial Cancer, 2008, v. 7, n. 1, p. 53, doi. 10.1007/s10689-007-9144-x
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- Publication type:
- Article
The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch Syndrome: from bench to bedside.
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- Familial Cancer, 2008, v. 7, n. 1, p. 41, doi. 10.1007/s10689-007-9145-9
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- Publication type:
- Article
Hereditary breast cancer: pathobiology, clinical translation, and potential for targeted cancer therapeutics.
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- Familial Cancer, 2008, v. 7, n. 1, p. 83, doi. 10.1007/s10689-007-9147-7
- Publication type:
- Article
Roles and responsibilities of a medical geneticist.
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- Familial Cancer, 2008, v. 7, n. 1, p. 5, doi. 10.1007/s10689-007-9148-6
- Publication type:
- Article